Recherche de Sous-structure

10651

CN1CCN(Cc2ccc(-c3cc4onc(-c5ccccc5)c4c(=O)n3C)cc2)CC1
Reaction #8404
5-methyl-6-[4-(4-methyl-piperazin-1-ylmethyl)-phenyl]-3-phenyl-5H-isoxazolo[4,5-c]pyridin-4-one
Rendement 41.2%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(-c2ccccc2)cc2noc(-c3ccccc3)c2c1=O
Reaction #8406
5-methyl-3,6-diphenyl-5H-isoxazolo[4,3-c]pyridin-4-one
Rendement 48.9%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)cc(N)c2cc(-c3ccc(Cl)cc3)c(-c3ccc(Cl)cc3Cl)nc21
Reaction #42083
4-Amino-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-1,8-naphthyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(=O)n(C)c2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc12
Reaction #42084
N-[6-(4-Chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1c[nH]c(=O)cc1-c1cc(Cl)ccc1[N+](=O)[O-]
Reaction #85018
4-(5-Chloro-2-nitrophenyl)-5-methoxypyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1cn(C(C)C(=O)O)c(=O)cc1-c1cc(Cl)ccc1[N+](=O)[O-]
Reaction #85019
2-[4-(5-Chloro-2-nitrophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1N(C)C(=O)CCNCCCOc1ccc2c(ccc(=O)n2C)c1
Reaction #156217
title compound
Rendement 50.8%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cccn(-c2ccc([N+](=O)[O-])cc2OC)c1=O
Reaction #172388
1-(2-Methoxy-4-nitrophenyl)-3-vinylpyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc([N+](=O)[O-])ccc1-n1cccc(CCO)c1=O
Reaction #172389
3-(2-Hydroxyethyl)-1-(2-methoxy-4-nitrophenyl)pyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc([N+](=O)[O-])ccc1-n1cccc(CCO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)c1=O
Reaction #172390
3-(2-{[tert-Butyl(diphenyl)silyl]oxy}ethyl)-1-(2-methoxy-4-nitrophenyl)pyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccnc2[nH]c(=O)c(CC(=O)N(CCNC(=O)OC(C)(C)C)CC(=O)O)cc12
Reaction #178088
DOI: 10.1039/C8SC04228D
COc1ccc(Cn2ccc(CCO)c([N+](=O)[O-])c2=O)cc1
Reaction #184922
DOI: 10.1039/C8SC04228D
Cc1cc(Br)cnc1CCCCNc1ncc(Cc2ccn(Cc3ccccc3)c(=O)c2)c(=O)[nH]1
Reaction #195911
DOI: 10.1039/C8SC04228D
O=C(Cn1cccc(OCc2ccccc2)c1=O)ON1C(=O)CCC1=O
Reaction #196358
DOI: 10.1039/C8SC04228D
CCCCn1ccc(Cc2cnc(NCCSCc3nc[nH]c3C)[nH]c2=O)cc1=O
Reaction #200245
DOI: 10.1039/C8SC04228D
COc1cc([N+](=O)[O-])ccc1-n1cccc(CCO)c1=O
Reaction #201065
DOI: 10.1039/C8SC04228D
CC(=O)c1ccc2c(c1)c1cc(-c3ccc(Cl)cc3Cl)c(=O)n(C)c1n2C(F)F
Reaction #206221
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(F)cc1)N1CCN(c2cc(=O)[nH]c3cc(Cl)ccc23)CC1
Reaction #206579
DOI: 10.1039/C8SC04228D
CC(=O)Nc1ccc2nc3c4ccccc4c(=O)n(-c4ccc(Cl)nc4)c3n2c1
Reaction #207210
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cnc2[nH]c(=O)ccc2c1Nc1ccc(OC)cc1
Reaction #215813
ethyl 4-[4-methoxyanilino]-7-oxo-7,8-dihydro-1,8-naphthyridine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
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